Canonical Allele Identifier: CA1451994760

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205657_39205658delinsGC , CM000666.2:g.39205657_39205658delinsGC	GRCh38
NC_000004.11:g.39207277_39207278delinsGC , CM000666.1:g.39207277_39207278delinsGC	GRCh37
NC_000004.10:g.38883672_38883673delinsGC	NCBI36
NG_031813.1:g.28254_28255delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.811_812delinsGC MANE Select	ENSP00000382717.3:p.Ala271=
ENST00000399820.7:c.811_812delinsGC	ENSP00000382717.3:p.Ala271=
ENST00000503697.5:c.*279_*280delinsGC	ENSP00000423706.1:n.*279_*280delinsGC
ENST00000506503.1:c.811_812delinsGC	ENSP00000423491.1:p.Ala271=
ENST00000506869.5:c.*392_*393delinsGC	ENSP00000424319.1:n.*392_*393delinsGC
ENST00000511729.5:n.41-22901_41-22900delinsGC
ENST00000512448.1:n.405_406delinsGC
NM_025132.3:c.811_812delinsGC	NP_079408.3:p.Ala271=
XM_011513724.1:c.811_812delinsGC	XP_011512026.1:p.Ala271=
XM_011513725.1:c.745_746delinsGC	XP_011512027.1:p.Ala249=
XM_011513726.1:c.331_332delinsGC	XP_011512028.1:p.Ala111=
XM_011513727.1:c.331_332delinsGC	XP_011512029.1:p.Ala111=
XM_011513728.1:c.331_332delinsGC	XP_011512030.1:p.Ala111=
XM_011513729.1:c.811_812delinsGC	XP_011512031.1:p.Ala271=
XR_925155.1:n.875_876delinsGC
NM_001317924.1:c.331_332delinsGC	NP_001304853.1:p.Ala111=
XM_011513725.2:c.745_746delinsGC	XP_011512027.1:p.Ala249=
XM_011513726.3:c.331_332delinsGC	XP_011512028.1:p.Ala111=
XM_017008501.1:c.331_332delinsGC	XP_016863990.1:p.Ala111=
XR_001741306.1:n.875_876delinsGC
XR_001741307.1:n.875_876delinsGC
XR_001741308.1:n.875_876delinsGC
XR_001741309.1:n.875_876delinsGC
XR_001741310.1:n.875_876delinsGC
XR_001741311.2:n.724_725delinsGC
XR_001741312.1:n.875_876delinsGC
NM_025132.4:c.811_812delinsGC MANE Select	NP_079408.3:p.Ala271=
NM_001317924.2:c.331_332delinsGC	NP_001304853.1:p.Ala111=